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Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway

The presence of gastric cancer stem cells (GCSCs) marks the onset of gastric carcinoma. The sonic hedgehog (SHH) pathway plays a vital role in the maintenance of GCSC characteristics. Apatinib has been approved in China for advanced gastric cancer (GC) treatment. However, whether apatinib can target...

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Autores principales: Cao, Wanshuang, Li, Yuan, Sun, Hongliang, Yang, Chenying, Zhu, Jianyun, Xie, Chunfeng, Li, Xiaoting, Wu, Jieshu, Geng, Shanshan, Wang, Lu, Sun, Liangfei, Geng, Guozhu, Han, Hongyu, Zhong, Caiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326764/
https://www.ncbi.nlm.nih.gov/pubmed/34350176
http://dx.doi.org/10.3389/fcell.2021.679806
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author Cao, Wanshuang
Li, Yuan
Sun, Hongliang
Yang, Chenying
Zhu, Jianyun
Xie, Chunfeng
Li, Xiaoting
Wu, Jieshu
Geng, Shanshan
Wang, Lu
Sun, Liangfei
Geng, Guozhu
Han, Hongyu
Zhong, Caiyun
author_facet Cao, Wanshuang
Li, Yuan
Sun, Hongliang
Yang, Chenying
Zhu, Jianyun
Xie, Chunfeng
Li, Xiaoting
Wu, Jieshu
Geng, Shanshan
Wang, Lu
Sun, Liangfei
Geng, Guozhu
Han, Hongyu
Zhong, Caiyun
author_sort Cao, Wanshuang
collection PubMed
description The presence of gastric cancer stem cells (GCSCs) marks the onset of gastric carcinoma. The sonic hedgehog (SHH) pathway plays a vital role in the maintenance of GCSC characteristics. Apatinib has been approved in China for advanced gastric cancer (GC) treatment. However, whether apatinib can target GCSCs and affect the SHH pathway remains unclear. The present study aimed to investigate the underlying mechanism of apatinib’s antitumor effects on GC. The expression levels of GCSC markers and number of CD133(+) cells were significantly elevated in the sphere-forming cells. Apatinib effectively suppressed GCSC traits by inhibiting tumorsphere formation and cell proliferation, suppressing GCSC markers expression and CD133(+) cell number, and inducing apoptosis. Apatinib downregulated the activation of the SHH pathway; while upregulation of the SHH pathway attenuated the inhibitory effects of apatinib on GCSCs. Moreover, apatinib treatment significantly delayed tumor growth and inhibited GCSC characteristics in the xenograft model. Our data suggested that apatinib exhibited inhibitory effects on GCSCs by suppressing SHH pathway both in vitro and in vivo, thus providing new insights into the therapeutic application of apatinib in GCSC suppression and advanced gastric cancer treatment.
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spelling pubmed-83267642021-08-03 Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway Cao, Wanshuang Li, Yuan Sun, Hongliang Yang, Chenying Zhu, Jianyun Xie, Chunfeng Li, Xiaoting Wu, Jieshu Geng, Shanshan Wang, Lu Sun, Liangfei Geng, Guozhu Han, Hongyu Zhong, Caiyun Front Cell Dev Biol Cell and Developmental Biology The presence of gastric cancer stem cells (GCSCs) marks the onset of gastric carcinoma. The sonic hedgehog (SHH) pathway plays a vital role in the maintenance of GCSC characteristics. Apatinib has been approved in China for advanced gastric cancer (GC) treatment. However, whether apatinib can target GCSCs and affect the SHH pathway remains unclear. The present study aimed to investigate the underlying mechanism of apatinib’s antitumor effects on GC. The expression levels of GCSC markers and number of CD133(+) cells were significantly elevated in the sphere-forming cells. Apatinib effectively suppressed GCSC traits by inhibiting tumorsphere formation and cell proliferation, suppressing GCSC markers expression and CD133(+) cell number, and inducing apoptosis. Apatinib downregulated the activation of the SHH pathway; while upregulation of the SHH pathway attenuated the inhibitory effects of apatinib on GCSCs. Moreover, apatinib treatment significantly delayed tumor growth and inhibited GCSC characteristics in the xenograft model. Our data suggested that apatinib exhibited inhibitory effects on GCSCs by suppressing SHH pathway both in vitro and in vivo, thus providing new insights into the therapeutic application of apatinib in GCSC suppression and advanced gastric cancer treatment. Frontiers Media S.A. 2021-07-19 /pmc/articles/PMC8326764/ /pubmed/34350176 http://dx.doi.org/10.3389/fcell.2021.679806 Text en Copyright © 2021 Cao, Li, Sun, Yang, Zhu, Xie, Li, Wu, Geng, Wang, Sun, Geng, Han and Zhong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Cao, Wanshuang
Li, Yuan
Sun, Hongliang
Yang, Chenying
Zhu, Jianyun
Xie, Chunfeng
Li, Xiaoting
Wu, Jieshu
Geng, Shanshan
Wang, Lu
Sun, Liangfei
Geng, Guozhu
Han, Hongyu
Zhong, Caiyun
Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway
title Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway
title_full Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway
title_fullStr Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway
title_full_unstemmed Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway
title_short Apatinib Suppresses Gastric Cancer Stem Cells Properties by Inhibiting the Sonic Hedgehog Pathway
title_sort apatinib suppresses gastric cancer stem cells properties by inhibiting the sonic hedgehog pathway
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326764/
https://www.ncbi.nlm.nih.gov/pubmed/34350176
http://dx.doi.org/10.3389/fcell.2021.679806
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